Abstract

An efficient data collection method is important for microcrystals, because microcrystals are sensitive to radiation damage. Moreover, microcrystals are difficult to harvest and locate owing to refraction effects from the surface of the liquid drop or optically invisible, owing to their small size. Collecting X-ray diffraction data directly from the crystallization devices to completely eliminate the crystal harvesting step is of particular interest. To address these needs, novel microplates combining crystal growth and data collection have been designed for efficient in situ data collection and fully tested at Shanghai Synchrotron Radiation Facility (SSRF) crystallography beamlines. The design of the novel microplates fully adapts the advantage of in situ technology. Thin Kapton membranes were selected to seal the microplate for crystal growth, the crystallization plates can support hanging drop and setting drop vapor diffusion crystallization experiments. Then, the microplate was fixed on a magnetic base and mounted on the goniometer head for in situ data collection. Automatic grid scanning was applied for crystal location with a Blu-Ice data collection system and then in situ data collection was performed. The microcrystals of lysozyme were selected as the testing samples for diffraction data collection using the novel microplates. The results show that this method can achieve comparable data quality to that of the traditional method using the nylon loop. In addition, our method can efficiently and diversely perform data acquisition experiments, and be especially suitable for solving structures of multiple crystals at room temperature or cryogenic temperature.

Highlights

  • In recent years, in order to efficiently obtain the structure of protein, various processing steps of the protein crystallography have been improved and optimized, especially with the development of in situ X-ray crystallography [1]

  • In addition to the development of in situ data collection methods, microcrystals are sensitive to radiation damage, so it is necessary to collect data from multiple crystals in a small wedge and integrate the diffraction images of multiple crystals into a full dataset

  • A typical result of the crystal growth under different crystallization conditions is shown in Figure 2e,f, which shows that crystallization conditions can be initially screened with microplate A and B under the microscope system (Figure 2e,f)

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Summary

Introduction

In order to efficiently obtain the structure of protein, various processing steps of the protein crystallography have been improved and optimized, especially with the development of in situ X-ray crystallography [1]. The method of in situ diffraction has been developed to directly collect datasets from the location where crystals were grown using X-ray diffraction, which eliminates the process of transferring the crystal sample to nylon loop and avoids the influence of human factors on the quality of the crystals. This method was originally used to screen crystals and verify the quality of crystals, but this method is mainly used to collect multiple data sets to obtain high-resolution protein structures, because in situ diffraction can greatly improve the efficiency of data collection, and at the same time, is very suitable for some special crystals. Thin films with high transparency can make the crystals visible on the microscope on the beamline station, which can efficiently locate the crystal position and facilitate data collection. (3) Chemical corrosion resistance; the crystal solution may contain corrosive components, or may chemically react with some thin film materials, resulting in the thin film materials being unusable. (4) Radiation resistance; synchrotron radiation X-ray has a high luminous flux, so the radiation dose is large, and the selected thin film material should be radiation resistant

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